FDA 510(k)

Vista Dyes

K-Number: K193447 · 2020-03-11

ApplicantInter-Med/Vista Dental Products

Decision Date2020-03-11

Product CodeLFC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Vista Dyes is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2020-03-11 under 510(k) number K193447. The device is classified under product code LFC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vista Dyes?

Vista Dyes is a medical device that received FDA 510(k) clearance on 2020-03-11. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K193447.

When did Vista Dyes receive FDA 510(k) clearance?

Vista Dyes received FDA 510(k) clearance on 2020-03-11, under 510(k) number K193447.

Who is the listed applicant for Vista Dyes?

The FDA 510(k) record lists Inter-Med/Vista Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vista Dyes?

The FDA product code for Vista Dyes is LFC.

Other records listing Inter-Med/Vista Dental Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K193357V-Mix K193409Vista Rinse, Vista Rinse Plus K193389Vista Clear K190220Vista FS, Vista FS Liquid K170101Valiant Curing Light

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K222560BlueCheck™ Caries Detection & MonitoringIncisive Technologies Pty, Ltd.K200601LumiCare Caries Diagnostic RinseGreenMark Biomedical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.